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Month of birth, vitamin D and risk of immune-mediated disease: a case control study

BACKGROUND: A season of birth effect in immune-mediated diseases (ID) such as multiple sclerosis and type 1 diabetes has been consistently reported. We aimed to investigate whether season of birth influences the risk of rheumatoid arthritis, Crohn's disease, ulcerative colitis and systemic lupu...

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Autores principales: Disanto, Giulio, Chaplin, George, Morahan, Julia M, Giovannoni, Gavin, Hyppönen, Elina, Ebers, George C, Ramagopalan, Sreeram V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395583/
https://www.ncbi.nlm.nih.gov/pubmed/22764877
http://dx.doi.org/10.1186/1741-7015-10-69
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author Disanto, Giulio
Chaplin, George
Morahan, Julia M
Giovannoni, Gavin
Hyppönen, Elina
Ebers, George C
Ramagopalan, Sreeram V
author_facet Disanto, Giulio
Chaplin, George
Morahan, Julia M
Giovannoni, Gavin
Hyppönen, Elina
Ebers, George C
Ramagopalan, Sreeram V
author_sort Disanto, Giulio
collection PubMed
description BACKGROUND: A season of birth effect in immune-mediated diseases (ID) such as multiple sclerosis and type 1 diabetes has been consistently reported. We aimed to investigate whether season of birth influences the risk of rheumatoid arthritis, Crohn's disease, ulcerative colitis and systemic lupus erythematosus in addition to multiple sclerosis, and to explore the correlation between the risk of ID and predicted ultraviolet B (UVB) light exposure and vitamin D status during gestation. METHODS: The monthly distribution of births of patients with ID from the UK (n = 115,172) was compared to that of the general population using the Cosinor test. Predicted UVB radiation and vitamin D status in different time windows during pregnancy were calculated for each month of birth and correlated with risk of ID using the Spearman's correlation coefficient. RESULTS: The distributions of ID births significantly differed from that of the general population (P = 5e(-12)) with a peak in April (odds ratio = 1.045, 95% confidence interval = 1.024, 1.067, P < 0.0001) and a trough in October (odds ratio = 0.945, 95% confidence interval = 0.925, 0.966, P < 0.0001). Stratification by disease subtype showed seasonality in all ID but Crohn's disease. The risk of ID was inversely correlated with predicted second trimester UVB exposure (Spearman's rho = -0.49, P = 0.00005) and third trimester vitamin D status (Spearman's rho = -0.44, P = 0.0003). CONCLUSIONS: The risk of different ID in the UK is significantly influenced by the season of birth, suggesting the presence of a shared seasonal risk factor or factors predisposing to ID. Gestational UVB and vitamin D exposure may be implicated in the aetiology of ID.
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spelling pubmed-33955832012-07-13 Month of birth, vitamin D and risk of immune-mediated disease: a case control study Disanto, Giulio Chaplin, George Morahan, Julia M Giovannoni, Gavin Hyppönen, Elina Ebers, George C Ramagopalan, Sreeram V BMC Med Research Article BACKGROUND: A season of birth effect in immune-mediated diseases (ID) such as multiple sclerosis and type 1 diabetes has been consistently reported. We aimed to investigate whether season of birth influences the risk of rheumatoid arthritis, Crohn's disease, ulcerative colitis and systemic lupus erythematosus in addition to multiple sclerosis, and to explore the correlation between the risk of ID and predicted ultraviolet B (UVB) light exposure and vitamin D status during gestation. METHODS: The monthly distribution of births of patients with ID from the UK (n = 115,172) was compared to that of the general population using the Cosinor test. Predicted UVB radiation and vitamin D status in different time windows during pregnancy were calculated for each month of birth and correlated with risk of ID using the Spearman's correlation coefficient. RESULTS: The distributions of ID births significantly differed from that of the general population (P = 5e(-12)) with a peak in April (odds ratio = 1.045, 95% confidence interval = 1.024, 1.067, P < 0.0001) and a trough in October (odds ratio = 0.945, 95% confidence interval = 0.925, 0.966, P < 0.0001). Stratification by disease subtype showed seasonality in all ID but Crohn's disease. The risk of ID was inversely correlated with predicted second trimester UVB exposure (Spearman's rho = -0.49, P = 0.00005) and third trimester vitamin D status (Spearman's rho = -0.44, P = 0.0003). CONCLUSIONS: The risk of different ID in the UK is significantly influenced by the season of birth, suggesting the presence of a shared seasonal risk factor or factors predisposing to ID. Gestational UVB and vitamin D exposure may be implicated in the aetiology of ID. BioMed Central 2012-07-06 /pmc/articles/PMC3395583/ /pubmed/22764877 http://dx.doi.org/10.1186/1741-7015-10-69 Text en Copyright ©2012 Disanto et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Disanto, Giulio
Chaplin, George
Morahan, Julia M
Giovannoni, Gavin
Hyppönen, Elina
Ebers, George C
Ramagopalan, Sreeram V
Month of birth, vitamin D and risk of immune-mediated disease: a case control study
title Month of birth, vitamin D and risk of immune-mediated disease: a case control study
title_full Month of birth, vitamin D and risk of immune-mediated disease: a case control study
title_fullStr Month of birth, vitamin D and risk of immune-mediated disease: a case control study
title_full_unstemmed Month of birth, vitamin D and risk of immune-mediated disease: a case control study
title_short Month of birth, vitamin D and risk of immune-mediated disease: a case control study
title_sort month of birth, vitamin d and risk of immune-mediated disease: a case control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395583/
https://www.ncbi.nlm.nih.gov/pubmed/22764877
http://dx.doi.org/10.1186/1741-7015-10-69
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